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FIGURE 2 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics

FIGURE 2. Thalictrum angustialatum in the wild (Qiaojia in Yunnan, China). A. Habitat. B. Habit (plant in flowering). C. Habit (plant in fruiting). D. Roots. E. Portion of stem. F. Leaf (left: adaxial side; right: abaxial side; inset: stipels). G. Leaflet (left: adaxial side; right: abaxial side). H. Flower. I. Sepal (left: abaxial side; right: adaxial side). J. Stamens. K. Carpels. L. Aggregate fruit. M. Achenes (immature). Photographed by Y.P. Zeng.

FIGURE 7 in Molecular and morphological evidences confirm the statuses of Ancistroides othonias (Hewitson, 1878) and the subspecies of A. nigrita (Latreille, [1824]), sensu Evans 1949 (Lepidoptera, Hesperiidae)

FIGURE 7. Male genitalia of Ancistroides armatus (A95). A. ring, lateral view; B. tegumen, dorsal view; C. gnathos, ventral view; D. uncus, dorsal view; E. left valva, inner side; F. left valva, dorsal view; G. aedeagus, dorsal view; H. aedeagus, lateral view; I. juxta.

FIGURE 4 in Molecular and morphological evidences confirm the statuses of Ancistroides othonias (Hewitson, 1878) and the subspecies of A. nigrita (Latreille, [1824]), sensu Evans 1949 (Lepidoptera, Hesperiidae)

FIGURE 4. Female genitalia of Ancistroides species. Codes correspond to the specimen IDs in Table 1 and Figure 1. A. lateral view; B. ventral view; C. lamella postvaginalis, front view.

FIGURE 1 in Molecular and morphological evidences confirm the statuses of Ancistroides othonias (Hewitson, 1878) and the subspecies of A. nigrita (Latreille, [1824]), sensu Evans 1949 (Lepidoptera, Hesperiidae)

FIGURE 1. NJ tree based on Kimura-2-Parameter distances for the partial mitochondrial COI sequences of Ancistroides, values at nodes represent the bootstrap support (BP) values.

FIGURE 3 in Molecular and morphological evidences confirm the statuses of Ancistroides othonias (Hewitson, 1878) and the subspecies of A. nigrita (Latreille, [1824]), sensu Evans 1949 (Lepidoptera, Hesperiidae)

FIGURE 3. Male genitalia of Ancistroides othonias (An13). A. ring, lateral view; B. uncus and gnathos, posterior view; C. tegumen, dorsal view; D. gnathos, ventral view; E. uncus, dorsal view; F. left valva, inner side; G. left valva, dorsal view; H. aedeagus, lateral view; I. aedeagus, dorsal view; J. juxta.

FIGURE 2 in Molecular and morphological evidences confirm the statuses of Ancistroides othonias (Hewitson, 1878) and the subspecies of A. nigrita (Latreille, [1824]), sensu Evans 1949 (Lepidoptera, Hesperiidae)

FIGURE 2. Adults of Ancistroides species. Codes correspond to the specimen IDs in Table 1 and Figure 1.

FIGURE 5 in Molecular and morphological evidences confirm the statuses of Ancistroides othonias (Hewitson, 1878) and the subspecies of A. nigrita (Latreille, [1824]), sensu Evans 1949 (Lepidoptera, Hesperiidae)

FIGURE 5. Male genitalia of Ancistroides nigrita nigrita (A97) and A. nigrita diocles (An4). A. ring, lateral view; B. tegumen, dorsal view; C. gnathos, ventral view; D. uncus, dorsal view; E. left valva, inner side; F. left valva, dorsal view; G. aedeagus, dorsal view; H. aedeagus, lateral view; I. juxta.

FIGURE 8 in Molecular and morphological evidences confirm the statuses of Ancistroides othonias (Hewitson, 1878) and the subspecies of A. nigrita (Latreille, [1824]), sensu Evans 1949 (Lepidoptera, Hesperiidae)

FIGURE 8. Male genitalia of Ancistroides longicornis (A96). A. ring, lateral view; B. uncus and gnathos, posterior view; C. tegumen, dorsal view; D. gnathos, ventral view; E. uncus, dorsal view; F. left valva, inner side; G. left valva, dorsal view; H. aedeagus, lateral view; I. aedeagus, dorsal view; J. juxta.

FIGURE. Strobilanthes glandulata. A in Strobilanthes glandulata (Acanthaceae), a new species from Sri Lanka based on the morphological and molecular evidences

FIGURE. Strobilanthes glandulata. A. Corolla split open showing the stamens; B. Inflorescence; C. Leaf; D. Flowering branch; E. Close up of the leaf surfaces.

FIGURE. Strobilanthes glandulata. A in Strobilanthes glandulata (Acanthaceae), a new species from Sri Lanka based on the morphological and molecular evidences

FIGURE. Strobilanthes glandulata. A. Habit; B. Flowering branch; C. Inflorescence; D & F. Leaves adaxial and abaxial view; E. front view of corolla; G. Internode; H. Bracts.

FIGURE. DnaSP DNA polymorphism analysis - Nucleotide variability (Pi) comparison between Strobilanthes lupulina and S. glandulata. The window length and step size were set to 600bp and 200bp respectively. The most varying regions and the commonly used barcoding regions are listed against the base-pair differences found. in Strobilanthes glandulata (Acanthaceae), a new species from Sri Lanka based on the morphological and molecular evidences

FIGURE. DnaSP DNA polymorphism analysis - Nucleotide variability (Pi) comparison between Strobilanthes lupulina and S. glandulata. The window length and step size were set to 600bp and 200bp respectively. The most varying regions and the commonly used barcoding regions are listed against the base-pair differences found.

FIGURE. Strobilanthes lupulina. A in Strobilanthes glandulata (Acanthaceae), a new species from Sri Lanka based on the morphological and molecular evidences

FIGURE. Strobilanthes lupulina. A. Flowering branch; B–C Inflorescence; D. Leaves adaxial and abaxial view; E. Bracts; F. Corolla split open showing the stamens; G. front view of corolla; H. Close up of the leaf surface; I. Stamens; J. Internode; K. Capsule.

FIGURE. Strobilanthes lupulina. A in Strobilanthes glandulata (Acanthaceae), a new species from Sri Lanka based on the morphological and molecular evidences

FIGURE. Strobilanthes lupulina. A. Capsule; B. Calyx; C. Bracts; D. Corolla split open showing the stamens; E. Inflorescences; F. Flowering branch; G. Close up of the leaf surfaces; H. Leaf.

FIGURE. Pollen morphology of S. glandulata and S. lupulina observed under SEM. A–C. Strobilanthes lupulina. A: Equatorial view, B, C: Exine ornamentation. D–F. Strobilanthes glandulata. D: Equatorial view, E, F: Exine ornamentation. in Strobilanthes glandulata (Acanthaceae), a new species from Sri Lanka based on the morphological and molecular evidences

FIGURE. Pollen morphology of S. glandulata and S. lupulina observed under SEM. A–C. Strobilanthes lupulina. A: Equatorial view, B, C: Exine ornamentation. D–F. Strobilanthes glandulata. D: Equatorial view, E, F: Exine ornamentation.

FIGURE 2 in A new species of Neoconidiobolus (Entomophthorales, Ancylistaceae) from China based on morphological, molecular and physiological evidences

FIGURE 2. Neoconidiobolus pseudothromboides sp. nov. RCEF 6692. A, Colony on PDA after 3 d at 21 ˚C; b, Mycelia rarely branched at the edge; c, Mycelia septate and distended like a block; d, e,f, Single primary conidiophores bearing a primary conidium; g, h, Primary conidia with small basal papilla; i, j, Secondary conidia producing from primary ones; k, Zygospores formed between segments of the same hyphae; l, Young zygospores; m, Mature zygospores. — Scale bars: a = 10 mm; b = 100 μm; c–m = 20 μm.

FIGURE 1 in A new species of Neoconidiobolus (Entomophthorales, Ancylistaceae) from China based on morphological, molecular and physiological evidences

FIGURE 1. Maximum Likelihood phylogenetic tree of Neoconidiobolus based on nucLSU, mtSSU and EFL sequences. Eight species in related genera (Azygosporus, Capillidium, Conidiobolus and Microconidiobolus) are chosen as outgroups. Maximum Parsimony bootstrap values (≧70%) / Maximum Likelihood bootstrap values (≧70%) / Bayesian Inference posterior probabilities (≧0.95) of each clade are indicated along branches. Neoconidiobolus pseudothromboides sp. nov. is shown in bold. Scale bar indicates substitutions per site.

FIGURE 3 in A new species and new records of Phlegmacium (Cortinariaceae) from China based on molecular and morphological evidence

FIGURE 3. (Continued) The basidiospores and pileipellis of P. paracephalixum: E1–4. HKAS92058; P. patrickense: F1–4. HKAS124259; P. violaceorubens: G1–4. HKAS124254.

FIGURE 3 in A new species and new records of Phlegmacium (Cortinariaceae) from China based on molecular and morphological evidence

FIGURE 3. The basidiospores and pileipellis of P. ochraceosquamosum: A1–4. HKAS124256 (holotype); P. caesiocolor: B1–4. HKAS67872; P. glaucopus: C1–4. HKAS124253; P. kytoevuorii: D1–4. HKAS124252. (continued on the next page)

FIGURE 2 in A new species and new records of Phlegmacium (Cortinariaceae) from China based on molecular and morphological evidence

FIGURE 2. Basidiomata of P. ochraceosquamosum: A1–2. HKAS124256 (holotype); P. caesiocolor: B. HKAS67872; P. glaucopus: C. HKAS124253; P. kytoevuorii: D. HKAS124252; P. paracephalixum: E. HKAS92058; P. patrickense: F. HKAS124259; P. violaceorubens: G. HKAS124254. Bars = 10 mm. Photos by Jian-Wei Liu (A1–2), Qing Cai (B, E), Geng-Shen Wang (C–D), Li-Rong Liu (F), Liu-Kun Jia (G).

FIGURE 1 in A new species and new records of Phlegmacium (Cortinariaceae) from China based on molecular and morphological evidence

FIGURE 1. Maximum-Likelihood phylogenetic tree inferred from the ITS dataset. Bootstrap values equal to or greater than 50% and Bayesian posterior probabilities equal to or greater than 0.95 are shown along the branches. Sequences generated in this study are in blue bold face.